ClinVar Miner

List of variants in gene combination SCN1A, SCN9A studied for Generalized epilepsy with febrile seizures plus, type 7

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Total variants: 17
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HGVS dbSNP
NM_001365536.1(SCN9A):c.1135A>G (p.Met379Val) rs544004654
NM_001365536.1(SCN9A):c.1280T>C (p.Leu427Ser) rs192406412
NM_001365536.1(SCN9A):c.1285C>T (p.Arg429Cys) rs763256222
NM_001365536.1(SCN9A):c.1314+1G>T rs1295192882
NM_001365536.1(SCN9A):c.1555G>A (p.Glu519Lys) rs187453572
NM_001365536.1(SCN9A):c.1744G>A (p.Glu582Lys) rs201391809
NM_001365536.1(SCN9A):c.1844A>G (p.Asn615Ser) rs780995899
NM_001365536.1(SCN9A):c.1921A>T (p.Asn641Tyr) rs121908918
NM_001365536.1(SCN9A):c.1997A>G (p.Lys666Arg) rs121908919
NM_001365536.1(SCN9A):c.2219T>C (p.Ile740Thr)
NM_001365536.1(SCN9A):c.2351C>G (p.Thr784Ser) rs200624920
NM_001365536.1(SCN9A):c.2461G>A (p.Val821Met) rs41268671
NM_001365536.1(SCN9A):c.3482G>A (p.Trp1161Ter) rs759003928
NM_001365536.1(SCN9A):c.4820C>T (p.Thr1607Ile) rs200470541
NM_001365536.1(SCN9A):c.5164C>T (p.Pro1722Ser)
NM_001365536.1(SCN9A):c.5704C>T (p.Arg1902Cys) rs200956485
NM_001365536.1(SCN9A):c.5750T>C (p.Ile1917Thr) rs200876442

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